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Journal Abstract Search

368 related items for PubMed ID: 14985786

  • 21. [Adeno-associated virus vector carrying human minidystrophin gene SMCKA3999 effectively ameliorates dystrophic pathology in mdx model mice].
    Li HH, Zhang SM, Fang SY, Chen CL, Luo YD, Guan Y, Wang DW, Xiao X.
    Zhonghua Yi Xue Za Zhi; 2003 Sep 10; 83(17):1513-6. PubMed ID: 14521733
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  • 23. Immune rejection of human dystrophin following intramuscular injections of naked DNA in mdx mice.
    Braun S, Thioudellet C, Rodriguez P, Ali-Hadji D, Perraud F, Accart N, Balloul JM, Halluard C, Acres B, Cavallini B, Pavirani A.
    Gene Ther; 2000 Sep 10; 7(17):1447-57. PubMed ID: 11001364
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  • 25. Gene delivery to dystrophic muscle.
    Wells KE, McMahon J, Foster H, Ferrer A, Wells DJ.
    Methods Mol Biol; 2008 Sep 10; 423():421-31. PubMed ID: 18370219
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  • 29. Mini- and full-length dystrophin gene transfer induces the recovery of nitric oxide synthase at the sarcolemma of mdx4cv skeletal muscle fibers.
    Decrouy A, Renaud JM, Lunde JA, Dickson G, Jasmin BJ.
    Gene Ther; 1998 Jan 10; 5(1):59-64. PubMed ID: 9536265
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  • 30. A canine minidystrophin is functional and therapeutic in mdx mice.
    Wang B, Li J, Qiao C, Chen C, Hu P, Zhu X, Zhou L, Bogan J, Kornegay J, Xiao X.
    Gene Ther; 2008 Aug 10; 15(15):1099-106. PubMed ID: 18432277
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  • 31. [Expression of the human dystrophin gene in mdx mouse muscle fibers after transfection using liposomes and synthetic oligopeptides].
    Baranov VS, Tarasenko OV, Baranov VS, Tarasenko OV, Baranov AN, Kiselev AV, Ivashchenko TE, Evgrafov OV, Mikhailov Vm, Dickson G.
    Genetika; 1998 Jul 10; 34(7):876-82. PubMed ID: 9749328
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  • 32. Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx mice.
    Ito K, Kimura S, Ozasa S, Matsukura M, Ikezawa M, Yoshioka K, Ueno H, Suzuki M, Araki K, Yamamura K, Miwa T, Dickson G, Thomas GD, Miike T.
    Hum Mol Genet; 2006 Jul 15; 15(14):2266-75. PubMed ID: 16777842
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  • 33. Intraperitoneal administration of phosphorothioate antisense oligodeoxynucleotide against splicing enhancer sequence induced exon skipping in dystrophin mRNA expressed in mdx skeletal muscle.
    Takeshima Y, Yagi M, Wada H, Matsuo M.
    Brain Dev; 2005 Oct 15; 27(7):488-93. PubMed ID: 16198206
    [Abstract] [Full Text] [Related]

  • 34. Codon optimization of the microdystrophin gene for Duchene muscular dystrophy gene therapy.
    Athanasopoulos T, Foster H, Foster K, Dickson G.
    Methods Mol Biol; 2011 Oct 15; 709():21-37. PubMed ID: 21194019
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  • 35. Electroporation of corrective nucleic acids (CNA) in vivo to promote gene correction in dystrophic muscle.
    Kapsa RM, Wong SH, Quigley AF.
    Methods Mol Biol; 2008 Oct 15; 423():405-19. PubMed ID: 18370218
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  • 36. Dmd(mdx-beta geo): a new allele for the mouse dystrophin gene.
    Wertz K, Füchtbauer EM.
    Dev Dyn; 1998 Jun 15; 212(2):229-41. PubMed ID: 9626497
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  • 37. Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs.
    Acsadi G, Dickson G, Love DR, Jani A, Walsh FS, Gurusinghe A, Wolff JA, Davies KE.
    Nature; 1991 Aug 29; 352(6338):815-8. PubMed ID: 1881437
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  • 38. The mechanism of naked DNA uptake and expression.
    Wolff JA, Budker V.
    Adv Genet; 2005 Aug 29; 54():3-20. PubMed ID: 16096005
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  • 39. Modular flexibility of dystrophin: implications for gene therapy of Duchenne muscular dystrophy.
    Harper SQ, Hauser MA, DelloRusso C, Duan D, Crawford RW, Phelps SF, Harper HA, Robinson AS, Engelhardt JF, Brooks SV, Chamberlain JS.
    Nat Med; 2002 Mar 29; 8(3):253-61. PubMed ID: 11875496
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  • 40. Factors influencing the efficacy, longevity, and safety of electroporation-assisted plasmid-based gene transfer into mouse muscles.
    Molnar MJ, Gilbert R, Lu Y, Liu AB, Guo A, Larochelle N, Orlopp K, Lochmuller H, Petrof BJ, Nalbantoglu J, Karpati G.
    Mol Ther; 2004 Sep 29; 10(3):447-55. PubMed ID: 15336645
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